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The benefits and challenges of family genetic testing in rare genetic diseases-lessons from Fabry disease.
Germain DP, Moiseev S, Suárez-Obando F, Al Ismaili F, Al Khawaja H, Altarescu G, Barreto FC, Haddoum F, Hadipour F, Maksimova I, Kramis M, Nampoothiri S, Nguyen KN, Niu DM, Politei J, Ro LS, Vu Chi D, Chen N, Kutsev S. Germain DP, et al. Among authors: barreto fc. Mol Genet Genomic Med. 2021 May;9(5):e1666. doi: 10.1002/mgg3.1666. Epub 2021 Apr 9. Mol Genet Genomic Med. 2021. PMID: 33835733 Free PMC article. Review.
Rare inherited kidney diseases: an evolving field in Nephrology.
Cunha MFMD, Sevignani G, Pavanelli GM, Carvalho M, Barreto FC. Cunha MFMD, et al. Among authors: barreto fc. J Bras Nefrol. 2020 Mar 20;42(2):219-230. doi: 10.1590/2175-8239-JBN-2018-0217. J Bras Nefrol. 2020. PMID: 32227072 Free PMC article.
Growth Differentiation Factor-15 and Syndecan-1 Are Potential Biomarkers of Cardiac and Renal Involvement in Classical Fabry Disease under Enzyme Replacement Therapy.
Gregório PC, Biagini G, Cunha RSD, Budag J, Martins AM, Rivas LV, Schiefer EM, Sánchez-Niño MD, Ortiz A, Stinghen AEM, Barreto FC. Gregório PC, et al. Among authors: barreto fc. Kidney Blood Press Res. 2022;47(4):229-238. doi: 10.1159/000521329. Epub 2022 Jan 27. Kidney Blood Press Res. 2022. PMID: 35086103 Free article.
Enzyme replacement therapy for Anderson-Fabry disease.
El Dib R, Gomaa H, Carvalho RP, Camargo SE, Bazan R, Barretti P, Barreto FC. El Dib R, et al. Among authors: barreto fc. Cochrane Database Syst Rev. 2016 Jul 25;7(7):CD006663. doi: 10.1002/14651858.CD006663.pub4. Cochrane Database Syst Rev. 2016. PMID: 27454104 Free PMC article. Review.
Renal Manifestations of Fabry Disease: A Narrative Review.
Silva CAB, Moura-Neto JA, Dos Reis MA, Vieira Neto OM, Barreto FC. Silva CAB, et al. Among authors: barreto fc. Can J Kidney Health Dis. 2021 Jan 19;8:2054358120985627. doi: 10.1177/2054358120985627. eCollection 2021. Can J Kidney Health Dis. 2021. PMID: 33786192 Free PMC article. Review.
97 results